Tobacco Center of Regulatory Science

**The Tobacco Center of Regulatory Science program concluded in 2024** 

Integrated Health, Behavioral and Economic Research on Current and Emerging Tobacco Products

The UCSF Center for Tobacco Control Research and Education was home to one of 9 Tobacco Centers of Regulatory Science (TCORS) supported by the U.S. Food and Drug Administration and the National Institutes of Health.  CTCRE Director, Professor Pamela Ling was Principal Investigator for this five-year $20 million project to study the impacts of new and emerging tobacco products, including e-cigarettes and heated tobacco products (HTPs), which heat tobacco without combustion.  The UCSF TCORS research projects, which were also be supported by $1 million in funding from UCSF, rangeed from the products' impacts on lung and cardiovascular disease to school-age usage and the impact on health care costs in general and vulnerable populations.

After decades of stability, the tobacco products people use and the way they use them are changing. Cigarette use continues to decline, but e-cigarette, cigar, and moist snuff use are increasing and use of multiple products is becoming more common.  New "heated tobacco products" are being proposed to the FDA as modified risk tobacco products.  There is only a limited evidence base to inform regulatory and public communication responses to these changes.  

The five main UCSF TCORS projects all shared three primary goals:

  1. Evaluate the short-term health effects of the new tobacco products and how specific product characteristics influence health effects and behavior
  2. Scientifically inform product standards and marketing regulations for the new products
  3. Build the tobacco regulatory science research community

9 TCORS

The TCORS accomplised these aims through 5 main projects, as well as developmental and rapid response projects and career enhancement.  The main projects were: 

UCSF TCORS 1.0: Improved Models to Inform Tobacco Product Regulation (2013-2018)

The first UCSF TCORS developed models to inform tobacco product regulation that integrated 1) economic impacts of tobacco use on healthcare costs, 2) risk perceptions, perceived acceptability, consumer responses to pro-tobacco marketing and anti-tobacco messages and other social determinants of tobacco use, and 3) rapid changes in risk due to tobacco use and secondhand smoke exposure as manifest in cardiovascular and pulmonary dysfunction. We had a particular focus on immediate effects of tobacco use and effects on susceptible populations (such as people exposed to infection) because these immediate effects have not been given adequate attention in the regulatory process. You can review a summary of our accomplishments that published 137 peer reviewed papers and 81 public comments to FDA and other agencies on tobacco regulations (as of October 2018) to speed dissmenation of our work.